Offer summary
Qualifications:
Bachelor's degree in life sciences or nursing, Previous experience as a CRA in ophthalmology, Strong knowledge of ophthalmic diseases and treatments, Understanding of clinical research regulations and GCP, Certification as CCRA or similar is a plus.
Key responsabilities:
- Assist in site selection and initiation for trials
- Conduct monitoring visits for data quality and compliance
- Ensure regulatory compliance across trial sites
- Verify subject qualification and investigational product handling
- Complete documentation and monitoring reports